Fu Yun-Feng, Zhu Yi-Na, Ni Jia, Zhong Xiang-Gen, Tang Wei, Zhou Ru, Zhou Yu, Dong Jia-Rong, He Pei-Lan, Wan Hua, Li Yuan-Chao, Yang Yi-Fu, Zuo Jian-Ping
Laboratories of Immunopharmacology and Medicinal Chemistry, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, People's Republic of China.
J Neuroimmunol. 2006 Jun;175(1-2):142-51. doi: 10.1016/j.jneuroim.2006.03.011. Epub 2006 May 19.
A novel triptolide derivative (5R)-5-hydroxytriptolide (LLDT-8) has been shown to have potent immunosuppressive activities. Here LLDT-8 was evaluated in experimental autoimmune encephalomyelitis (EAE), the model of multiple sclerosis (MS). LLDT-8 reduced the incidence and severity of EAE, which was associated with the inhibition of the MOG 35-55 lymphocyte recall response, anti-MOG 35-55 T cell responses, interleukin (IL)-2 and interferon (IFN)-gamma production. In vitro, LLDT-8 inhibited primary T cells proliferation, division, IL-2 and IFN-gamma production stimulated with anti-CD3/28. These findings highlight the fact that LLDT-8 prevents EAE by suppressing T cell proliferation and activation, with a potential for treatment of MS.
一种新型雷公藤内酯醇衍生物(5R)-5-羟基雷公藤内酯醇(LLDT-8)已被证明具有强大的免疫抑制活性。在此,LLDT-8在实验性自身免疫性脑脊髓炎(EAE)——多发性硬化症(MS)模型中进行了评估。LLDT-8降低了EAE的发病率和严重程度,这与抑制MOG 35-55淋巴细胞回忆反应、抗MOG 35-55 T细胞反应、白细胞介素(IL)-2和干扰素(IFN)-γ的产生有关。在体外,LLDT-8抑制了抗CD3/28刺激的原代T细胞增殖、分裂、IL-2和IFN-γ的产生。这些发现突出了LLDT-8通过抑制T细胞增殖和激活来预防EAE的事实,具有治疗MS的潜力。